Details for New Drug Application (NDA): 220232
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The generic ingredient in EMTRICITABINE, RILPIVIRINE AND TENOFOVIR DISOPROXIL FUMARATE is emtricitabine; rilpivirine hydrochloride; tenofovir disoproxil fumarate. There are eighteen drug master file entries for this compound. Three suppliers are listed for this compound. Additional details are available on the emtricitabine; rilpivirine hydrochloride; tenofovir disoproxil fumarate profile page.
Summary for 220232
| Tradename: | EMTRICITABINE, RILPIVIRINE AND TENOFOVIR DISOPROXIL FUMARATE |
| Applicant: | Laurus |
| Ingredient: | emtricitabine; rilpivirine hydrochloride; tenofovir disoproxil fumarate |
| Patents: | 0 |
Suppliers and Packaging for NDA: 220232
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| EMTRICITABINE, RILPIVIRINE AND TENOFOVIR DISOPROXIL FUMARATE | emtricitabine; rilpivirine hydrochloride; tenofovir disoproxil fumarate | TABLET;ORAL | 220232 | ANDA | Laurus Labs Limited | 42385-801 | 42385-801-30 | 30 TABLET, FILM COATED in 1 BOTTLE (42385-801-30) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 200MG;EQ 25MG BASE;300MG | ||||
| Approval Date: | Mar 4, 2026 | TE: | AB | RLD: | No | ||||
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